Flow-i 麻醉系統,Flow-c 麻醉系統,Flow-e 麻醉系統
K 號:K191027 · 2020-03-18
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器材摘要
常見問題
What is the Flow-i Anesthesia System, Flow-c Anesthesia System, Flow-e Anesthesia System?
Flow-i Anesthesia System, Flow-c Anesthesia System, Flow-e Anesthesia System is a medical device that received FDA 510(k) clearance on 2020-03-18. The listed applicant is Maquet Critical Care AB. The 510(k) number is K191027.
When did Flow-i Anesthesia System, Flow-c Anesthesia System, Flow-e Anesthesia System receive FDA 510(k) clearance?
Flow-i Anesthesia System, Flow-c Anesthesia System, Flow-e Anesthesia System received FDA 510(k) clearance on 2020-03-18, under 510(k) number K191027.
Who is the listed applicant for Flow-i Anesthesia System, Flow-c Anesthesia System, Flow-e Anesthesia System?
FDA 510(k) 記錄將 Maquet Critical Care AB 列為申請人。這並不單獨確立設備製造商。
What is the FDA product code for Flow-i Anesthesia System, Flow-c Anesthesia System, Flow-e Anesthesia System?
The FDA product code for Flow-i Anesthesia System, Flow-c Anesthesia System, Flow-e Anesthesia System is BSZ.
相關臨床試驗
相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係,請查閱連結的官方來源。
其他以 Maquet Critical Care AB 為申請人之記錄
相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係,請查閱連結的官方來源。
相關器械(代碼:BSZ)
相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係,請查閱連結的官方來源。
官方來源
在 FDA 資料庫中查看 →資料來源為 FDA Open API。如需最新且權威的資訊,請始終參閱官方記錄。
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